Class IITerminated in FDA datasetRecall initiated Jul 9, 2019

DaVinci Laboratories of Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex

Recalling firm: FoodScience Corporation

Why it was recalled

Dietary supplement mislabeled, undeclared allergen.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 11, 2019.

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ProductDaVinci Laboratories of Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex, 60 count UPC Code 026664273161
UPC026664273161

FDA code information

Lot Code: 35532200 EXP: 05/2022

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Full FDA record and distribution details

Original product description

DaVinci Laboratories of Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex, 60 count UPC Code 026664273161

Extracted codes and context

TypeCode / valueContext
UPC026664273161 Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex, 60 count UPC Code 026664273161
lot35532200Lot Code: 35532200 EXP: 05/2022

Original FDA recall reason

Dietary supplement mislabeled, undeclared allergen.

Recall details

Recall number
F-1595-2019
Event ID
83292
FDA status
Terminated
Initiated
Jul 9, 2019
Reported
Jul 31, 2019
Classified
Jul 23, 2019
Terminated
Oct 11, 2019
Quantity
256 bottles
Location
Williston, VT, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

Product distributed to customers in the following states: PA< IN, CA, NH, VT, MD, MI, MN, NY, LA, CT, OR, MO, AZ, OH, FL, KS, IL. There is one International customer in Tokyo, Japan.

FDA source record · F-1595-2019

Data updated September 16, 2026. View official FDA data ↗

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